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![Page 1: Open Access Full Text Article Arm port vs chest port: a ......This article was published in the following Dove Press journal: Cancer Management and Research Guanhua Li1,* Yu Zhang](https://reader033.vdocuments.site/reader033/viewer/2022052006/6019df682c0d6824ca4cac74/html5/thumbnails/1.jpg)
OR I G I N A L R E S E A R C H
Arm port vs chest port: a systematic review and
meta-analysisThis article was published in the following Dove Press journal:
Cancer Management and Research
Guanhua Li1,*
Yu Zhang2,*
Hongmin Ma3
Junmeng Zheng1
1Department of Cardiovascular Surgery,
Sun Yat-sen Memorial Hospital, Sun Yat-
sen University, Guangzhou, Guangdong
510120, People’s Republic of China;2Department of Pathology, The Second
Affiliated Hospital of Guangzhou
University of Chinese Medicine,
Guangdong Provincial Hospital of
Chinese Medicine, Guangzhou,
Guangdong 510120, People’s Republic of
China; 3Department of Surgery,
Guangzhou Women and Children’sMedical Center, Guangzhou, Guangdong
510623, People’s Republic of China
*These authors contributed equally to
this work
Background: Two prevailing, totally implantable venous access ports are routinely utilized
in oncology: chest port or arm port. This systematic review with meta-analysis
was conducted to compare safety and efficiency of the two techniques.
Methods: We performed evidence acquisition intensively from PubMed, Embase, and
Cochrane Library. Available comparative studies that evaluated both techniques were identi-
fied. The outcomes of interest included total complication events, procedure-related infec-
tions, thrombosis, intra-operative complications, mechanical complications, conversion rate,
early port removal, and operating time.
Results: Thirteen comparative studies including 3,896 patients (2,176 for chest ports, and
1,720 for arm ports) were identified. The present study showed that arm port was associated
with higher procedure conversion rate (2.51% in chest port group and 8.32% in arm port
group; odd ratios [OR] 0.27, 95% confidence interval [CI] 0.15-0.46; p<0.001), but lower
incidence of intra-operative complications (1.38% in chest port group and 0.41% in arm port
group; OR 2.38, 95% CI 1.07–5.29; p=0.03). There were no between-group differences with
respect to total complication events, procedure-related infections, thrombosis, mechanical
complications, early port removal, and operating time. Subgroup analysis of patients under
60 years revealed that no significant difference was detected in intra-operative events (1.19%
in chest port group and 0.02% in arm port group, OR 2.59, 95% CI 0.74–9.08; p<0.14),
indicating that age may be a risk factor for intra-operative events. Sensitivity analysis did not
change conclusions of all endpoints of interest.
Conclusion: Arm port is associated with higher procedure conversion rate, but lower incidence
of intra-operative complications, and age may be a risk factor for intra-operative events.
Keywords: chest port, arm port, total implantable venous access port, systematic review,
meta-analysis
IntroductionTotally implantable venous access ports (TIVAPs), a long-term indwelling infusion
system, was first introduced by Niederhuber in 1982.1 With the increasing use of
chemotherapeutic drugs in oncologic patients, TIVAP gains its popularity due to the
fact that this system enables long-term administration of chemotherapeutic agents,
attenuates the burden of chemotherapy, and thus greatly improves quality of life in
oncologic patients, meanwhile, this system preserves peripheral vessels and prevents
venous-related infections.2–4 Two prevailing approaches are routinely utilized in
oncology: chest ports or arm ports. Chest ports are most frequently implanted
under the guidence of ultrasonography, via internal jugular vein, external jungular
vein or subclavian vein puncture, while arm ports are placed through forearm veins
such as basilic vein, cephalic vein or brachial vein, either through percutaneous
Correspondence: Junmeng ZhengDepartment of Cardiovascular Surgery, SunYat-sen Memorial Hospital, Sun Yat-senUniversity, No.107 Yanjiang West Road,Guangzhou 510120, People’s Republic ofChinaTel +86 208 133 2603Fax +86 208 133 2853Email [email protected]
Cancer Management and Research Dovepressopen access to scientific and medical research
Open Access Full Text Article
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and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the workyou hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. Forpermission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
http://doi.org/10.2147/CMAR.S205988
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puncture or surgical cut-down, both generally showing
satisfactory results with respect to technical success and
low incidence of postprocedural complications.5,6
For years, the chest has been the most popular and
reliable access site of implantation for long-term indwelling
ports, however, chest ports might not be eligible for patients
undergoing radiotherapy with chest wall involvement, or
those with chest wall skin lesions, meanwhile, many female
patients experience perception of “foreign body”, “bra
inconvenience”, and discomfort when wearing safety belt
or bag strap. In 1993, an alternative arm port procedure was
introduced by surgeons at the School of Medicine, Yale
University.7 The arm ports have some unique advantages
compared with chest ports, such as no risk for hemothorax
or pneumothorax, lower incidence of arterial puncture,8
better cosmetic outcome,9 and more “bra convenience”.10
These advantages are especially beneficial to breast cancer
patients requiring radiotherapy, flap transferring for recon-
structive surgeries, as well as those patients with radioder-
matitis or compromised respiratory function.11
Nevertheless, the most significant disadvantage of arm
port implantation is high incidence of failure (technically
unsuccessful port placement), which is around 6.4%.12,13
Despite the wide application of TIVAPs, there is no
consensus whether one or the other access site of implanta-
tion for TIVAP is clinically superior. Although several stu-
dies that compared chest access and arm access had been
reported by various institutions, some of the results are con-
flicting and within small population of patients.14–16 In the
present study, we attempted to investigate and assemble the
most comprehensive clinical data currently available in
the literature to address a debatable issue: which approach,
the arm port or the chest port, is more clinically beneficial to
oncologic patients for the implantation of TIVAPs?
Evidence acquisitionClinical data search strategyThe present study was carried out according to the Meta-
analysis Of Observational Studies in Epidemiology
(MOOSE) recommendations and the Preferred Reporting
Items for Systematic Reviews and Meta-Analyses
(PRISMA) protocol.17,18 Systematic review registration was
not available. Literature search was executed in August 2018,
regardless of article types, regions or language of publication.
Eligible studies were primarily from on-line databases of
PubMed, Embase, and the Cochrane Library. Medical
Subject Headings (MeSH) terms, as well as their combinations
were manually searched via (Title/Abstract) as follows: basi-
lic/cephalic/brachial/subclavian/jugular AND totally implan-
table venous access port/totally implantable venous access
device/venous port/indwelling port, with “Related Articles”
function applied to expand the search results. Corresponding
author was contacted if additional information was required.
When the same group of authors published multiple but simi-
lar reports of studies, the most comprehensive or the most
recent result was taken into consideration.
Inclusion and exclusion criteriaInclusion criteria: 1) patients: patients who were diagnosed
with malignancies requiring long-term indwelling ports, or
those with gastrointestinal disorders requiring long-term
venous port for parenteral nutrition support; 2) intervention:
arm ports (basilic/cephalic/brachial vein insertion) vs chest
ports (subclavian or jugular vein insertion), regardless of
implantation methods, including surgical cut-down (peripheral
vein cut-down method through surgical approach) and percu-
taneous puncture (radiology-guided placement, ultrasound-
guided implantation, fluoroscopy-guided insertion, direct punc-
ture, and so forth); 3) study types: all randomized controlled
trials (RCTs), comparative studies available in the literature
including cohort and case control studies which compared
arm ports and chest ports were included; 4) outcomes: studies
quantitatively reporting at least one of the outcomes described
in the next section of this paper were included.
Exclusion criteria: 1) letters to the editor, editorials,
reviews, case reports, laboratory-based animal studies,
non-clinical studies, conference abstracts, and meta-
analysis papers; 2) studies that failed to clearly clarify
the outcomes of interest were excluded. If multiple access
sites of implantation were compared in a single study
(cephalic, jugular and subclavian vein), results of chest
port/arm port category were combined.
Data extractionTwo independent authors (YZ, GL) conducted data extraction.
Any discrepancy was resolved by discussion and consultation
with senior authors in this paper (HM and JZ). Data on clinical
characteristics (age, diagnosis), type of port, and technique
used (approach of insertion) were collected. Port-related com-
plications were classified into four categories: intra-operative
complications, infectious complications, thrombotic complica-
tions, and mechanical complications.19,20
The primary outcomes of interest were the incidences of
port-related complications from implantation to removal of
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TIVAP. Intra-operative complications included arterial punc-
ture, hemothorax, and pneumothorax. Procedure-related
infections, composed of port-site infection and catheter-
related bloodstream infection, were diagnosed in accordance
with the latest guideline of the Infectious Diseases Society of
America.21 Procedure-related thrombotic complications
were identified as any mural thrombi formed from the port
catheter to the vessel lumen, giving rise to catheter occlusion,
regardless of the presence of symptoms.22 On the basis of
Clavien-Dindo classification of surgical complications,23
mechanical complications included port misfunctioning
(such as deficiency of infusion or catheter occlusion), cathe-
ter fracture (defined as physical damage to the catheter of the
port system), port dislocation (also named catheter migration
or malposition), pinch-off syndrome, and hemorrhage.
The second outcomes of interest were conversion to other
access site of placement, early port removal (port removal
before completion of treatment), and operating duration.
Quality assessmentEvaluation of RCT quality was subject to the Cochrane
Collaboration’s tool, through which risk of bias was
assessed based on Cochrane Handbook for Systematic
Reviews of Interventions.24 Judgment of overall risk of
bias for each included RCT was assessed as: low, moder-
ate, or high.24 RCTs with low risk of bias were regarded as
high quality. Quality of observational study was assessed
according to the Newcastle-Ottawa scale (NOS), consist-
ing of three aspects: patient selection, comparability of the
study groups, and assessment of outcome.25 A quality
score ≥8 points was regarded as high quality study.
Statistical analysisReview Manager 5.0 (Cochrane Collaboration, Oxford,
UK) was used for this systematic review with meta-
analysis. Weighted mean difference (WMD) was used to
compare continuous variables, while odd ratio (OR) was
employed to compare dichotomous variables. Ninety-five
percent confidence interval (CI) was applied to all data
throughout this study. When confronting with continuous
variable expressed as mean and range value, standard
deviation (SD) was converted as suggested by Hozo
et al.26
Chi-squared test was used for the evaluation of statis-
tical heterogeneity between studies, and significance level
was set at p=0.10. For quantitative assessment of hetero-
geneity, I2 statistic was used, and high heterogeneity level
was set at 75%.27 The random-effects model was applied if
between-study heterogeneity was high, in order to make
more conservative estimates,28 otherwise, the fixed-effects
model was employed.24
Subgroup analyses were carried out for the outcomes of
intra-operative complications, thrombotic complications,
infectious complications, and mechanical complications.
Available data were stratified based on patient’s age, method
of placement (puncture or surgical cut-down), whether anti-
biotic or thromboprophylaxis was applied, so as to investi-
gate whether these factors influenced the outcomes.
Sensitivity analysis was performed and only outcomes with
at least two studies were included. We performed sensitivity
analysis for high quality studies (RCT with low risk of bias
and non-randomized studies with quality score ≥8 points).
We also used funnel plots to screen potential publication bias.
A two-tailed p-value less than 0.05 was considered as statis-
tical significance, except otherwise specified.
ResultsA total of 914 possibly eligible studies were identified
from databases (Figure 1). Thirteen studies including
3,896 cases (2,176 for chest ports, and 1,720 for arm
ports) fulfilled the inclusion standard and were selected
for final evidence synthesis. Agreement with respect to
study selection between the two reviewers was 92%.
Characteristics of included studiesTable 1 depicts the characteristics of included studies in this
study. Of these included studies, two29,30 were RCTs, and
Pubmed: n=287
Studies identified throughinitial searches of electronic
databases: n=914
Embase: n=564
Titles and abstracts screened:
Duplications: n=308
Excluded studies: n=582
Excluded studies: n=11
Meeting abstracts: n=4Reviews: n=5
Clinical trial description: n=2
Irrelevant atricles: n=476Non-comparative studies: n=15Animal studies: n=1Case reports: n=90
Full-text articles screened:
Included studies:n=13
n=606
n=24
Cochrane:n=63
Figure 1 Flow diagram of study selection process.
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Tab
le1Characteristicsofincludedstudies
Study
Yea
rCountry
Design
Patients
Appro
ach
forCP
Appro
ach
forAP
Antibiotic
Coag
ulation
Match
ing
Age
,
years(m
ean/
med
ian)
Ran
geCP
AP
TIVAP
Pro
phy
laxis
Pro
phy
laxis
Alahyaneetal32
2010
Morroco
RC
43
16–76
340
240
NR
NR
NR
NR
Yes
NR
Akahaneetal33
2011
Japan
RC
64
20–91
47
115
P-U
Celsite
Puncture/
ultrasound
Puncture/
radiological
None
NR
1,2,4,5,7,8,9
Biffietal29
2009
Italy
RCT
52
18–75
270
133
Bardport
Puncture/
ultrasound
Surgicalcut-
down
NR
None
1,2,4,5,6,7
D'Angelo
etal30
2002
Italy
RCT
61.5
17–75
25
25
NR
Puncture/
ultrasound
Surgicalcut-
down
NR
NR
1,2,4,7
Goltzetal34
2012
Germ
any
RC
58.8
18–88
52
152
PowerPort
Puncture/
radiological
Puncture/
radiological
Yes
NR
1,2,4,5,7,8
Goltzetal10
2013
Germ
any
PC
55.8
19–84
25
25
PowerPort/P.
A.S
Port
Puncture/
radiological
Puncture/
radiological
NR
NR
1,2,4,5,7
Kuriakose
etal35
2002
USA
RC
58
14–88
273
149
BardPort/
Meditec-
R-Port
Puncture/
NR
Puncture/
radiological
NR
Yes
1,2,4,5,6,7,9
Lietal36
2016
People's
Republic
of
China
RC
53.6
NR
237
107
Bardport
Puncture/
direct
Puncture/
ultrasound
NR
NR
1,2,4,5,7
Marcy
etal37
2005
France
RC
55.7
NR
100
100
Bard/
BraunMedical
Surgicalcut-
down
Puncture/
radiological
None
NR
1,2,4,5,7,8
Marcy
etal38
2008
France
RC
59
20–83
112
113
Bard/
BraunMedical
Surgicalcut-
down
Puncture/
radiological
None
None
1,2,4,5,7,8,9
Matiotti-Neto
etal39
2017
USA
RC
NR
NR
247
195
NR
Puncture/
fluoroscopy
Surgicalcut-
down
NR
NR
1,2,3,4,5,6,7
Iorioetal31
2018
Italy
PC
59.5
NR
106
109
NR
Surgicalcut-
down
Surgicalcut-
down
Yes
NR
1,2,4,5,6,7,8
Shionoetal40
2014
Japan
RC
62.9
NR
342
257
BardX-Port/
Slim
Port
Puncture/
fluoroscopy
Puncture/
fluoroscopy
Yes
NR
1,2,4,5,7,8
Notes:
Matchingcriteria:1=age;2=sex;3=bodymassindex;4=TIVAPprocedure;5=primarymalignancy;6=sideofplacement;7=singlesurgicalorradiologist
team
;8=antibiotics
description;9=coagulationdescription.
Abbreviations:
RC,retrospectivecohort;PC,prospectivecohort;RCT,randomizedcontrolledtrial;CP,chest
port;AP,arm
port;NR,notreported;TIVAP,totally
implantable
venousaccess
port.
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two10,31 were prospective non-randomized cohort studies.
The remaining studies32-40 were retrospective. As for indica-
tions, the majority of included studies were about cancer
patients with upcoming chemotherapies, and most of the
reported studies used commercial venous port devices
(BardPort, PowerPort, P-U Celsite, BraunMedical, and
Meditec-R-Port). For port implantation, the majority of stu-
dies used percutaneous puncture approach, while there were
three studies31,37,38 and four studies29,31,39 which used direct
surgical cut-down methods to implant chest port devices and
arm port devices, respectively.
Based on Cochrane Handbook for Systematic Reviews
of Interventions,24 Table 2 summarizes the risk of bias of
two included RCTs, one RCT was considered as moderate
risk, while the other p< was regarded as low risk. In Table
3, risk of bias analysis of the remaining included studies
was summarized in line with the NOS.25 Among these
non-randomized studies, two32,39 had a quality score
below seven, and the remaining studies were considered
as high-quality.
Primary outcomesThe pooled data from 13 studies10,29–40 that evaluated
primary outcomes in 3,896 patients (Figure 2) revealed
no significant differences for total complication events
between the chest port and arm port groups (11.8% and
12.8%; OR 0.94, 95% CI 0.77–1.15; p=0.53). Eleven
studies in which 3,266 patients were included thoroughly
reported the incidences of intra-operative complications,
thrombotic complications, infectious complications, and
mechanical complications. For procedure-related infec-
tions, no statistically significant differences were observed
between the chest port and arm port groups (3.15% and
3.37%; OR 1.11, 95% CI 0.74–1.66; p=0.63). Differences
for procedure-related thrombotic complications and
mechanical complications were also absent between the
two groups (2.87% and 3.91%; OR 0.75, 95% CI
0.49–1.13; p=0.17; and 4.86% and 2.96%; OR 1.34, 95%
CI 0.92–1.95; p=0.13, respectively). However, when
comparing the difference for intra-operative complica-
tions, the incidence in chest port group was significantly
higher (1.38% and 0.41%; OR 2.38, 95% CI 1.07–5.29;
p=0.03) (Figure 3).
Secondary outcomesData on procedure conversion rate were obtained in six
studies,26,29,31,38–40 which assessed 1,314 and 914 patients in
chest port group and arm port group, respectively. The proce-
dure conversion rate was significantly higher in arm port group
than that in chest port group (2.51% in chest port group and
8.32% in arm port group; OR 0.27, 95% CI 0.15–0.46;
p<0.001) (Figure 4A). When incidences of early port removal
were analyzed, there were three studies29,36,39 including 1,189
patients evaluated, and no significant difference was present
between groups (7.29% and 4.37%; OR 1.27, 95% CI
0.26–6.19; p=0.77) (Figure 4A). As for operating time, three
studies including 707 patients were reported, however, one
study30 presented operating time as “mean ± standard devia-
tion”, one study39 presented as “mean and range”, and the last
one31 displayed as “mean and interquartile range”. Using
Hozo’s26 method, ranges were converted to estimated SD for
further comparison.41 Result of the analysis of operating time
revealed that there were no statistically significant differences
between chest port group and arm port group (WMD −4.31;95% CI −17.81–9.19; p=0.53), with high between-study het-
erogeneity (I2=0.98, p<0.01) (Figure 4B).
Subgroup analysisIn subgroup analysis of antibiotic prophylaxis, there were
no statistically significant differences with respect to infec-
tion rate in comparison of the previous results, suggesting
that prophylactic administration of antibiotics did not
interfere with procedure-related infection rate (Table 4).
Three studies29,35,38 reported the anticoagulant profiles,
and results showed that thromboprophylaxis did not influ-
ence the risk for thrombosis either. In the subgroup analy-
sis of insertion methods, only one study31 used surgical
cut-down approach in all patients, and six studies10,33–36,40
Table 2 Risk of bias of included randomized controlled trials based on Cochrane Handbook for Systematic Reviews of Interventions
Study Sequence
generation
Allocation
concealment
Blinding Incomplete
outcome data
Selective out-
come reporting
Other
sources of
bias
Risk of
bias
D'Angelo et al, 200230 Yes Uncertain Uncertain Yes Yes Yes Moderate
Biffi et al, 200929 Yes Yes Uncertain Yes Yes Yes Low
Notes: Low risk: 5–6 sections with “yes”; moderate risk: 3–4 sections with “yes”; high risk: ≤2 sections with “yes”.
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employed puncture approach for all patients. The results
did not change the conclusions for the primary outcomes
from original analyses, and pooled data from six studies
including 1,781 patients who underwent percutaneous
puncture approach indicated consistent results showing
that the incidences of intra-operative events in chest port
group were significantly higher (2.05% and 0.12%, OR
7.87, 95% CI 1.82–34.13; p<0.01) (Table 4). Finally, two
subgroups were stratified according to patients’ age group
(<60 years old and ≥60 years old). After pooling data from
eight studies including 2,063 patients less than 60 years
old, the result showed that no significant difference was
detected with regard to intra-operative events between
chest ports and arm ports (1.19% and 0.02%, OR 2.59,
95% CI 0.74–9.08; p<0.14), suggesting that age may be
a risk factor for intra-operative events (Table 4).
Sensitivity analysis and publication biasOne low risk RCT29 and six non-randomized comparative
studies10,33,35–38 that scored over eight points according to
NOS were included in the sensitivity analysis. The results
of sensitivity analysis did not change the conclusions for
total complication events, all of the primary outcomes, and
incidence of procedure conversion from original analyses.
However, between-study heterogeneity decreased slightly
in all of these parameters (Table 5). Due to insufficient
data, sensitivity analyses for early port removal and oper-
ating time were not performed.
Figure 5 depicts a funnel plot of included studies that
assessed primary outcomes of interest. The distribution was
even and around the vertical. Most of the studies were within
the 95% CIs, suggesting no apparent publication bias.
DiscussionThis systematic review with meta-analysis compared the
clinical efficacy of two types of TIVAPs: chest port and
arm port. Our results showed that arm port is a safe site for
implantation, with lower incidence of intra-operative com-
plications, however, arm port is associated with higher
procedure conversion rate. No statistically significant dif-
ferences between chest port and arm port were found in
total complication events, procedure-related infections,
procedure-related thrombotic complications, incidence of
early port removal, and operating duration. On subgroup
analysis, we found that antibiotic prophylaxis and method
of insertion did not interfere with the conclusions for the
primary outcomes from original analyses, but results
revealed that there were no statistically significantTab
le3Riskofbiasforincludednon-randomizedstudiesbasedonNewcastle-O
ttaw
ascale
Study
Rep
resentative
ness
oftheex
posed
cohort
Selec
tion
ofthe
non-
exposed
cohort
Ascertainmen
t
ofex
posu
re
Dem
onstrationthat
outcomeofinterest
was
notpresentat
startofstudy
Comparab
ility
ofco
hortson
thebasis
ofthe
designor
analysis
Assessm
ent
ofoutcome
Was
follo
w-
uplong
enough
for
outcomes
to
occur
Adeq
uac
y
offollo
w-
upof
cohorts
Quality
score
Alahyaneetal,201032
11
01
21
00
6
Akahaneetal,201133
11
11
21
11
9
Goltzetal,201234
11
11
21
00
7
Goltzetal,201310
11
11
21
11
9
Kuriakose
etal,200235
11
11
21
10
8
Lietal,201636
11
11
21
11
9
Marcy
etal,200537
11
11
21
11
9
Marcy
etal,200838
11
11
21
10
8
Matiotti-Neto
etal,201739
11
11
11
00
6
Iorioetal,201831
11
11
21
00
7
Shionoetal,201440
11
11
21
00
7
Notes:Qualityofobservationalstudyisassessedaccordingto
Newcastle-O
ttaw
ascale(N
OS),consistingofthreecomponents:patientselection(4
points),comparability
ofthestudygroups(2
points)andassessmentofoutcome(3
points).
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differences in intra-operative events in those patients under
60, suggesting that age may affect the risk for intra-
operative complications. Sensitivity analysis did not
change the conclusions of all endpoints of interest.
For the utilization of a new technique, patients’ safety
is always the first priority. Chest ports are still popular and
their application is continuously expanding among non-
surgical physicians.15 Under the guidance of ultrasound or
fluoroscopy, the risks for intra-operative events, such as
pneumothorax, hemothorax, and arterial injury, are there-
fore minimized during percutaneous cannulations of sub-
clavian vein or jugular vein.42 Implantation of arm ports
through peripheral forearm vessels is more surgically chal-
lenging, but arm port users experience less perception of
“foreign body”, with satisfactory cosmetic results. Pooled
data from 2,176 chest port and 1,720 arm port users from
included studies of this study, showed that incidences for
total complication events were 11.8% and 12.8%, respec-
tively. Our result of total complication events is in agree-
ment with previous studies that assessed overall
complication rate,4,19,43 with no significant difference
between chest ports and arm ports. Although the technique
of implanting arm ports is newly developed, and more
challenging for clinicians, our findings indicate that arm
ports are at least as safe as conventional chest ports with
proper patient indications.
The procedure conversion rate is significantly higher for
arm ports as compared to chest ports. Additional challenges
for arm port implantation include anatomic variations,
longer distance for implantation, and frequent use of per-
ipheral intravenous access, which make cannulation of per-
ipheral forearm vessels not always achievable. Anatomic
variations of basilic, cephalic or brachial vein frequently
occur, and these peripheral vessels are much smaller in
diameter as compared with central veins. These peripheral
forearm vessels may be difficult to recognize or too limited
in size to use.44 Therapeutic usage of peripheral venous
access is frequent for oncologic and critically-ill patients,
however, frequent puncture of these vessels leads to adhe-
sion, spasm, or shrinkage, and thus complicates anatomy of
surrounding structures. Moreover, patients with conversion
might reveal higher risks for other complications. As
implantation of indwelling TIVAPs is performed not only
by surgeons, but also widely performed by non-surgical
practitioners (such as trained physicians, radiologists,
anesthesiologists, oncologists, and so forth), arm port
implantation may need to be placed in selected patients to
avoid procedure conversion. In our experience, no matter
how experienced the clinician is in arm port implantation,
preoperative ultrasound evaluation of forearm vessels is
indicated in every case to minimize this unfavorable event.
Our findings showed that chest port was associated
with higher incidence of intra-operative complications.
Due to specific anatomy, accidental pneumothorax or
arterial puncture could not be eliminated completely,
even if ultrasound or fluoroscopy guidance is routinely
available. But interestingly, in subgroup analysis, no
between-group differences in intra-operative events were
seen in those patients under 60. Patients’ age appeared to
be relevant to the risk for intra-operative events, although
it is still poorly illustrated. Similar results were previously
reported: high age is an independent risk factor for proce-
dural complications in subclavian vein puncture, and one
implication is closely related to variations in body
Figure 2 Forest plot and meta-analysis of total complication events.
Abbreviation: M-H, Mantel-Haenszel method.
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habitus.45,46 Based on our experiences, our explanation is
that vessel fragility and decreased vessel elasticity may be
responsible for this issue, as the elderly are prone to
compromised vascular compliance, which makes the
aged population more susceptible to vascular interference
and trauma. Another potential reason is higher morbidities
of chronic obstructive pulmonary diseases and obesity that
attribute to structural elevation of apex pulmonis, thereby
Figure 3 Forest plot and meta-analysis of primary outcomes.
Abbreviation: M-H, Mantel-Haenszel method.
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facilitating the occurrence of pneumothorax.46 Certainly,
special caution in terms of intra-operative complications in
aged patients is alerted when performing implantation of
chest ports.
The pooled analyses of procedure-related infections,
thrombolytic complications, and mechanical complica-
tions showed no between-group differences. Subgroup
analysis of antibiotic prophylaxis demonstrated that
administration of antibiotics did not affect the outcome
of overall infection rate. But we still recommend that
anti-septic protocols should be followed for the sake of
infection prevention and management in oncologic
patients who are vulnerable to infection owing to leu-
kocytopenia induced by immune suppression.47
Subgroup analysis of thromboprophylaxis did not alter
any original conclusion, which was consistent with
Chaukiyal’s result48 showing that thromboprophylaxis
had no beneficial effects on the risks of catheter-
related thrombolytic complications in oncologic patients.
Nonetheless, as regular heparin flushing has become
routine practice for TIVAPs in almost every
institution,49 it seems to be enough for the prevention
of port-related thrombosis.50
Two methods of implanting TIVAPs are used in current
clinical practice: surgical cut-down or percutaneous punc-
ture. No consensus has ever been reached regarding implan-
tation methods because percutaneous puncture is less time-
consuming, but surgical cut-down method lowers the risk
for complications such as pneumothorax.31 With the world-
wide spread of ultrasound monitoring for venous access,
venous surgical cut-down method is on the decrease.31 No
significant difference in terms of insertion approach could
be addressed in this study. Of the three included studies in
which operating time was reported, detailed procedure
description was not available in one study,30 one study31
inserted TIVAPs through surgical cut-down, and the last39
separately used surgical approach and puncture to cannulate
arm ports and chest ports, respectively. Because of the
heterogeneous characteristic and data insufficiency, it is
difficult to reach a definite conclusion for the comparison
of inserting methods in this instance.
Arm port implantation is especially attractive to young
females for cosmetic reasons, as it leaves no scars on the
chest. Arm port users experience less “bra inconvenience”,
and psychologically, patients’ anxiety of indwelling arm
ports might be less as compared to chest ports.40
Figure 4 Forest plot and meta-analysis of secondary outcomes. (A) Comparison of procedure conversion rate and early port removal. (B) Comparison of operating time
between groups.
Abbreviations: M-H, Mantel-Haenszel method; IV, inverse variance method.
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Tab
le4Subgroupanalysiscomparingchest
portsandarm
ports
Gro
up
Pro
cedure-related
infections
Pro
cedure-related
thro
mbotic
complic
ations
Intra-operativeev
ents
Mec
han
ical
complic
ations
nOR(95%
CI)
I2 (%)
Heteroge
neity
nOR(95%
CI)
I2 (%)
Heteroge
neity
nOR(95%
CI)
I2 (%)
Heteroge
neity
nOR(95%
CI)
I2 (%)
Heteroge
neity
Ove
rall
11
1.11
(0.74–1.66)
00.59
11
0.75
(0.49–1.13)
28
0.19
11
2.38
(1.07–5.29)
36
0.17
11
1.34
(0.92–1.95)
25
0.21
Antibiotic
pro
phy
laxis
Yes
31.12
(0.56–2.24)
00.74
N/A
N/A
N/A
No
31.24
(0.55–2.76)
00.52
N/A
N/A
N/A
Anti-coag
ulant
pro
phy
laxis
Yes
N/A
10.91
(0.21–3.85)
N/
A
N/A
N/A
N/A
No
N/A
20.54
(0.12–2.32)
74
0.05
N/A
N/A
Methodof
insertion
Surgicalcut-down
10.51
(0.05–5.70)
N/
A
N/A
13.11
(0.13–77.29)
N/
A
N/A
10
N/
A
N/A
10
N/
A
N/A
Puncture
61.03
(0.63–1.68)
00.51
60.81
(0.42–1.56)
19
0.29
67.87
(1.82–34.13)
00.93
61.55
(0.98–2.47)
38
0.15
Age
<60yearsold
80.90
(0.54–1.52)
00.6
80.78
(0.50–1.23)
35
0.15
82.59
(0.74–9.08)
44
0.17
81.14
(0.75–1.74)
00.51
>60yearsold
21.25
(0.61–2.54)
00.8
21.00
(0.22–4.52)
N/
A
N/A
29.81
(1.13–85.37)
00.84
21.47
(0.03–71.26)
79
0.03
Abbreviations:
n,numberofstudies;N/A,notapplicable.
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Moreover, arm port is especially appropriate for patients
who require neck or chest radiation therapies.40
Comparison of these quality-of-life related outcomes is
of importance, however, only a limited number of studies
reported these parameters, which were measured based on
various evaluating methods, such as self-administered
questionnaire10,36 and quality of life score,37,46 and non-
uniformity of these measurements made these data incom-
parable in this study.
Our study is distinctive and provides valuable informa-
tion to oncology-related clinicians in that, to the best of our
knowledge, this systematic review with meta-analysis is the
first one to comprehensively investigate the clinical efficacies
and represents the most up-to-date information with respect
to chest ports and arm ports. We used multiple strategies to
launch evidence acquisition, strict standards to assess quality
of included studies, scientific statistics for data analysis,
subgroup and sensitivity analysis to control study heteroge-
neity. Our study has several limitations which should be
taken into consideration. First of all, the most apparent lim-
itation of the present study is that most of the included data
were from retrospective cohort studies. Inadequacy of rando-
mization and lack of blinding will increase the risk of bias.
Secondly, this study was based on the premised assumption
that demographic subgroups (age, sex, race, nationality, and
disease distribution) were similar enough for comparison.
However, subgroup analysis with regard to age generated
some different outcomes, hence, further systematic reviews
should be conducted when sufficient future results are
released. And then, the included studies were from different
institutions with various levels of clinician expertise. Not
only the between-study time-span, which is more than 10
Table 5 Sensitivity analysis comparing chest ports and arm ports
Outcome of interest Number
of studies
Number of chest
port patients
Number of arm
port patients
OR (95%CI) p-value I2
(%)
Heterogeneity
Total complication events 7 1,064 742 0.88 (0.67–1.17) 0.38 41 0.12
Procedure-related
infections
7 1,064 742 0.95 (0.56–1.62) 0.86 0 0.49
Procedure-related
thrombotic complications
7 1,064 742 0.92 (0.56–1.51) 0.74 34 0.18
Intra-operative events 7 1,064 742 3.28 (1.03–10.40) 0.04 33 0.21
Mechanical complications 7 1,064 742 1.06 (0.71–1.58) 0.79 0 0.52
Conversion rate 3 619 353 0.33 (0.19–0.57) <0.001 0 0.44
Figure 5 Funnel plot demonstrating meta-analysis of primary outcomes of interest.
Abbreviation: SE, standard error.
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years, but also the different backgrounds of the TIVAP
operators with different insertion approaches will affect the
outcomes of interest. Next, some outcomes of interest, espe-
cially the mechanical complications, might not be clearly
defined in some studies, yielding misinterpretation of results
or data omission. So, the incidence of mechanical complica-
tions might be underrated, and caution should be taken when
interpreting results of this section. Finally, follow-up period
of included studies was generally short. But there are increas-
ing cumulative risks for TIVAP-related infection, thrombo-
sis, and mechanical mis-functioning along with the duration
of port indwelling, some incidences of outcomes might be
underestimated because of insufficient follow-up period.
Surely, long-term outcomes of arm ports, especially for
oncologic efficacy and safety, require further investigation.
ConclusionIn this systematic review with meta-analysis that
compared clinical efficacy of two types of TIVAPs: chest
port and arm port, we found that arm port is associated with
higher procedure conversion rate, but lower incidence of intra-
operative complications. There are no statistically significant
differences between chest port and arm port with regard to in
total complication events, procedure-related infections, proce-
dure-related thrombotic complications, incidence of early port
removal, and operating duration. Age may be a risk factor for
intra-operative complications. Further confirmation of these
results is warranted and our findings should be updated with
larger scale and well-designed studies with longer follow-up.
AcknowledgmentThis study received no specific grant from any funding
agency.
DisclosureThe authors report no conflicts of interest in this work.
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DovePressCancer Management and Research 2019:116112